Variant report

Variant	rs1115519
Chromosome Location	chr4:80413011-80413012
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10021556	1.00[ASN][1000 genomes]
rs10022309	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10022314	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10027904	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10033410	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1031005	0.91[JPT][hapmap]
rs1074134	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11098741	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11098742	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11098770	0.90[JPT][hapmap]
rs1115518	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11736348	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11936123	0.94[ASN][1000 genomes]
rs12501981	0.86[CEU][hapmap];0.87[JPT][hapmap]
rs12502224	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12506212	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12510204	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12510243	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12511890	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12513177	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12639996	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12640638	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12643491	0.90[JPT][hapmap]
rs13111877	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13118924	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13146986	0.85[CEU][hapmap];0.90[JPT][hapmap]
rs1371996	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1440860	0.92[ASN][1000 genomes]
rs1440861	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1440862	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1440863	0.94[ASN][1000 genomes]
rs1440865	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1561638	0.94[ASN][1000 genomes]
rs1561639	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1561640	0.94[ASN][1000 genomes]
rs1595966	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1899232	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1971838	0.91[ASN][1000 genomes]
rs2119419	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2119420	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2119421	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3943669	0.90[JPT][hapmap]
rs4975052	0.94[ASN][1000 genomes]
rs4975053	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4975054	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4975055	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4975089	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs723243	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs723245	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7655446	0.94[ASN][1000 genomes]
rs7663844	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7670107	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7684683	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7690520	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7691021	0.94[ASN][1000 genomes]
rs7691868	1.00[ASN][1000 genomes]
rs7691918	1.00[ASN][1000 genomes]
rs7697359	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs880988	1.00[ASN][1000 genomes]
rs9307532	0.92[ASN][1000 genomes]
rs9307545	0.90[JPT][hapmap]
rs998437	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9993773	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999174	chr4:80212935-80512356	Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv3432913	chr4:80274683-80416584	Weak transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv879506	chr4:80316417-80604625	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv879507	chr4:80365765-80552199	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv879508	chr4:80398708-80552199	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:80412600-80413400	Enhancers	Gastric	stomach
2	chr4:80413000-80413200	Enhancers	ES-WA7 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links